SHC1
From Wikipedia, the free encyclopedia
SHC-transforming protein 1 is a protein that in humans is encoded by the SHC1 gene.[1] SHC has been found to be important in the regulation of apoptosis and drug resistance in mammalian cells.
SCOP classifies the 3D structure as belonging to the SH2 domain family.
References
- ↑ Pelicci G, Lanfrancone L, Grignani F, McGlade J, Cavallo F, Forni G, Nicoletti I, Grignani F, Pawson T, Pelicci PG (Aug 1992). "A novel transforming protein (SHC) with an SH2 domain is implicated in mitogenic signal transduction". Cell 70 (1): 93–104. doi:10.1016/0092-8674(92)90536-L. PMID 1623525.
Further reading
- Sasaoka T, Kobayashi M (2000). "The functional significance of Shc in insulin signaling as a substrate of the insulin receptor.". Endocr. J. 47 (4): 373–81. doi:10.1507/endocrj.47.373. PMID 11075717.
- Ravichandran KS (2001). "Signaling via Shc family adapter proteins.". Oncogene 20 (44): 6322–30. doi:10.1038/sj.onc.1204776. PMID 11607835.
- van der Geer P (2002). "Phosphorylation of LRP1: regulation of transport and signal transduction.". Trends Cardiovasc. Med. 12 (4): 160–5. doi:10.1016/S1050-1738(02)00154-8. PMID 12069755.
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